Lactobacillus gene engineering subunit vaccine strain capable of stably expressing porcine rotavirus VP4 protein and preparation method of lactobacillus gene engineering subunit vaccine strain
A porcine rotavirus and subunit vaccine technology, applied in the field of medicine, can solve problems such as biological safety hazards, instability of plasmid expression, loss of plasmids, etc., and achieve good immunogenicity
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Embodiment 1
[0053] The selection of embodiment 1 porcine rotavirus VP4 gene insertion site
[0054] Lactobacillus casei were respectively inoculated in MRS liquid medium containing 1% of different carbon sources (glucose, fructose, sucrose, galactose, lactose, trehalose, raffinose, polyfructose), and the total RNA of the bacteria was extracted for cheese Microarray analysis of the whole genome of Lactobacillus, and hierarchical clustering analysis of the microarray detection results to find genes that can be efficiently and stably expressed in different carbon source media. It has been detected that pyruvate hydratase gene RNA can be stably transcribed at a high level in different carbon sources. In order to obtain the recombinant Lactobacillus casei that expresses porcine rotavirus VP4 protein constitutively and efficiently in the genome, the present invention uses the pyruvate hydratase gene site as the recombination site of the VP4 gene, and inserts the stop codon of the pyruvate hydra...
Embodiment 2
[0055] Embodiment 2 Determination of the SD sequence containing the signal peptide sequence
[0056] The signal peptide sequence and ribosome binding site of peptidoglycan hydrolase were predicted by bioinformatics software SignalP-4.0. Using the Lactobacillus casei genome as a template to amplify the SD sequence containing the signal peptide sequence of the peptidoglycan hydrolase, the results are shown in figure 1 As shown, a fragment with a size of about 100 bp was obtained, the nucleotide sequence of which was shown in SEQ ID NO.1, and the fragment was ligated into the cloning vector pUC-57.
Embodiment 3
[0057] Example 3 Preparation of Recombinant Lactobacillus casei with Genome Constitutive High Expression of Porcine Rotavirus VP4 Protein
[0058] 1. Construction of gene targeting plasmid backbone
[0059] (1) Cloning of porcine rotavirus VP4 gene
[0060] Using the cDNA of the porcine rotavirus VP4 gene as a template and using VP4-F / VP4-R as primers, the porcine rotavirus VP4 gene fragment was amplified by PCR, and its nucleotide sequence was shown in SEQ ID NO.2. And at the two ends of the VP4 gene, restriction enzyme sites Pst I and Spe I were added, and the gene was connected to the pMD18-T vector. The primer sequences are shown in Table 1, and the PCR identification results are shown in figure 2 shown.
[0061] Table 1 Primer Sequence
[0062]
[0063]
[0064] (2) Subcloning of upstream and downstream recombinant homology arms
[0065] Using the genome of Lactobacillus casei as a template and using EB-F / EB-R and EA-F / EA-R as primers respectively, the upper an...
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